Memoona Ramzan

Also affiliated with University of Miami, University of the Punjab, Dr. John T. Macdonald Foundation, National Institute on Deafness and Other Communication Disorders

NeuroscienceBiochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 7 papers. Top paper: “Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan”.

Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan

Scientific Reports(2020)10.1038/s41598-020-68779-5

N/A

0DataRank · unranked

15 citations

Rasheeda Bashir, Midhat Salman, Ghulam Mujtaba, Nara Sobreira, P. Dane Witmer +2 more

Variants of human CLDN9 cause mild to profound hearing loss

Human Mutation(2021)10.1002/humu.24260

N/A

0DataRank · unranked

6 citations

Christophe Philippe, Inna A. Belyantseva, Yoko Nakano, Cristina Fenollar‐Ferrer, Risa Tona +19 more

Dispersed DNA variants underlie hearing loss in South Florida’s minority population

Human Genomics(2023)10.1186/s40246-023-00556-7

N/A

0DataRank · unranked

11 citations

Joanna Gonzalez, Dayna Morel Swols, Duygu Duman, Turçin Saridogan, Memoona Ramzan +11 more

Extreme Phenotypic Variability of ACTG1‐Related Disorders in Hearing Loss

Advanced Genetics(2024)10.1002/ggn2.202400040

N/A

0DataRank · unranked

2 citations

Memoona Ramzan, L.A. Calderón, Franco Salvatore, Maria Agustina De Rosa, Stephanie Bivona +12 more

Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2

European Journal of Human Genetics(2024)10.1038/s41431-024-01562-6

N/A

0DataRank · unranked

6 citations

Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Özgül M. Alper +9 more

Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63563

N/A

0DataRank · unranked

1 citations

Memoona Ramzan, Aslı Subaşıoğlu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan +7 more

Carboxypeptidase D deficiency causes hearing loss amenable to treatment

Journal of Clinical Investigation(2025)10.1172/jci192090

N/A

0DataRank · unranked

1 citations

Natalie Ortiz-Vega, Mohammad Faraz Zafeer, Amanda G. Lobato, Tahir Atık, Clemer Abad +25 more